Trial · NCT03360539
Outcomes60
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
41 to 60 of 60
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| SECONDARY | Number of Participants Experiencing Child Mortality | Within 24 months after index birth; Mortality records | Differs from randomized sample as it excludes participants who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With Recommended Number of Well-child Visits | At 15 months after index birth; Medicaid claims | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With Lead Screening | At 15 months after index birth; Medicaid claims | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With Developmental Screening | At 12 months after index birth; Medicaid claims | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With a Dental Visit | Within 24 months after index birth; Medicaid claims and dental records | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With Fluoride Treatment | Within 24 months after index birth; Medicaid claims and dental records | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With an Inter-birth Interval of < 24 Months | Within 24 months after index birth; vital records | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With an Inter-birth Interval of < 15 Months | Within 15 months after index birth; vital records | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Inter-birth Interval | 60 months after index birth; vital records | |||
| SECONDARY | Number of Participants With a Family Planning Visit (6 Weeks) | Within 6 weeks after index birth; Medicaid claims, hospital discharge | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants Who Received a Highly or Moderately Effective Method of Contraception (6 Weeks) | Within 6 weeks after index birth; Medicaid claims, hospital discharge | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants Who Received Immediate Postpartum Long-acting Reversible Contraception (6 Weeks) | Within 6 weeks after index birth; Medicaid claims, hospital discharge | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With a Family Planning Visit (1 Year) | Within 12 months after index birth; Medicaid claims, hospital discharge | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants Who Received a Highly or Moderately Effective Method of Contraception (1 Year) | Within 12 months after index birth; Medicaid claims, hospital discharge | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants Who Received a Postpartum Intrauterine Device Insertion (1 Year) | Within 12 months after index birth; Medicaid claims, hospital discharge | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Time to First Take-up of Family Planning Counseling or Service | Within 24 months after index birth; Medicaid claims, hospital discharge | Differs from randomized sample as it excludes participants with missing outcome data, an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | months | MEAN |
| SECONDARY | Time to First Take-up of Highly Effective Contraceptive Method | Within 24 months after index birth; Medicaid claims, hospital discharge | Differs from randomized sample as it excludes participants with missing outcome data, an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | months | MEAN |
| SECONDARY | Number of Participants Who Received Supplemental Nutrition Assistance Program (SNAP) or Special Supplemental Nutrition Program for Women, Infants, and Children (WIC) Benefits | During index pregnancy, assessed up to 42 weeks; South Carolina Department of Social Services data and birth certificate data respectively | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Months Receiving SNAP or Temporary Assistance for Needy Families (TANF) Benefits | Within 24 months after index birth; South Carolina Department of Social Services data | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | number of months | MEAN |
| SECONDARY | Number of Participants With SNAP or TANF Benefit Churn | Within 24 months after index birth; South Carolina Department of Social Services data | Differs from randomized sample as it excludes participants with an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy. | Participants | COUNT_OF_PARTICIPANTS |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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GET https://conductscience.org/api/trials/v1/NCT03360539/outcomes?page=3